Washington, DC (Remote) · 18d ago
Mission Regulatory Affairs Member
Excelya · posted Nov 4, 2026
Open to candidates in Bulgaria
Contract · Mid-level
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What this job asks for
Extracted by RemoteHuntMust have
- •3+ years of experience in Regulatory Affairs
- •Familiarity with Bulgarian regulatory requirements
- •Experience in EU regulatory submissions
- •Fluent in English and Bulgarian
- •Degree in Life Sciences
Nice to have
- •Experience with pharmaceutical companies or consultancies
Languages required
bg
Read the full posting
Redefine Regulatory Affairs. Empower Innovation. Build with Audacity.
Join Excelya as Our Next RA Star!
At Excelya , we don’t just work—we Excelyate . Across 24 countries, 900+ passionate professionals are shaping the future of healthcare with one bold ambition: to become Europe's leading mid-size CRO, offering the best employee experience .
Now, we’re calling on curious minds and courageous spirits to step into a career-defining role in Regulatory Affairs . Ready to make an impact that travels the globe? Let’s talk.
About the Job
We are seeking a Freelancer Mission Regulatory Affairs Member, based in Bulgaria for a part-time, full remote role, to provide scientific expertise required for the successful completion of Excelya’s projects.
Your Mission:
- To identify and communicate new Bulgarian legislation, amendments, guidelines and upcoming regulatory developments.
- To provide expert input on Bulgarian regulatory requirements.
- To manage EU regulatory submissions (DCP / MRP / National procedures).
- To be responsible for the review and approval of:
o Mock-ups (artwork review)
o Translation of Product information texts
o Promotional materials in compliance with local regulations
What You Bring to the Table:
We are looking for candidates who embody our values of Audacity, Care, and Energy and also:
- Degree in Life Sciences.
- At least 3 years of experience in Regulatory Affairs.
- Strong familiarity with local Regulatory requirements(as per Bulgarian Medicines Authority etc.) for pharmaceutical products for human use and medical devices.
- Experience in EU regulatory submissions (DCP / MRP / National procedures).
- Good understanding of EU regulatory framework and local regulations in Bulgaria.
- Detail-oriented with strong compliance mindset.
- Experience working with pharmaceutical companies or regulatory consultancies.
- Able to work independently and deliver high-quality results within tight timelines.
- Fluent in English and Bulgarian language.
Why Choose Excelya?
At Excelya, we lead with Audacity , act with Care , and move with Energy . We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger .
So, if you're ready to excel with purpose , let’s write the next chapter together.
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